(Q28268909)

8

Akira Kinoshita

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Koh-ichiro Yoshiura

9

Koh-ichiro Yoshiura

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Tohru Ohta

10

Tohru Ohta

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Tatsuya Kishino

11

Tatsuya Kishino

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Mutsuo Ishikawa

12

Mutsuo Ishikawa

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Yoshimitsu Fukushima

14

Yoshimitsu Fukushima

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author name string

Junichi Kamimura

1

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Keiko Wakui

2

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Hiroko Kadowaki

3

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Yukio Watanabe

4

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Kazuaki Miyake

5

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Naoki Harada

6

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Michiyo Sakamoto

7

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Masato Kasuga

13

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Naomichi Matsumoto

Journal of Human Genetics

16

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language of work or name

English

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publication date

2004

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published in

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volume

49

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issue

7

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page(s)

360-5

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cites work

Position effect in human genetic disease

1 reference

12 December 2020

Analysis of the gene sequences of the insulin receptor and the insulin-sensitive glucose transporter (GLUT-4) in patients with common-type non-insulin-dependent diabetes mellitus

1 reference

12 December 2020

Insulin receptor substrate-1 variants in non-insulin-dependent diabetes

1 reference

12 December 2020

Adolescent onset Type 2 diabetes in a non-obese Caucasian patient with an unbalanced translocation

1 reference

12 December 2020

Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene

1 reference

12 December 2020

Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region.

1 reference

12 December 2020

Purified inositol hexakisphosphate kinase is an ATP synthase: diphosphoinositol pentakisphosphate as a high-energy phosphate donor

1 reference

12 December 2020

A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity

1 reference

12 December 2020

Synthesis of diphosphoinositol pentakisphosphate by a newly identified family of higher inositol polyphosphate kinases

1 reference

12 December 2020

HNF-1alpha G319S, a transactivation-deficient mutant, is associated with altered dynamics of diabetes onset in an Oji-Cree community

1 reference

12 December 2020

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

1 reference

12 December 2020

Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p

1 reference

12 December 2020

Mutation in the calcium-binding domain of the mitochondrial glycerophosphate dehydrogenase gene in a family of diabetic subjects

1 reference

12 December 2020

Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects

1 reference

12 December 2020

The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetes

1 reference

12 December 2020

Nonsense and missense mutations in the human hepatocyte nuclear factor-1 beta gene (TCF2) and their relation to type 2 diabetes in Japanese

1 reference

12 December 2020

Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus

1 reference

12 December 2020

Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain

1 reference

12 December 2020

Variability of the pancreatic islet beta cell/liver (GLUT 2) glucose transporter gene in NIDDM patients

1 reference

12 December 2020

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

12 December 2020

Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.

1 reference

12 December 2020

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus

1 reference

12 December 2020